CaCO₃ nanoparticles as an ultra-sensitive tumor-pH-responsive nanoplatform enabling real-time drug release monitoring and cancer combination therapy

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• 作者：Ziliang Dong^a ; Liangzhu Feng^a ; ^{liangzhu.f@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Wenwen Zhu^a ; Xiaoqi Sun^a ; Min Gao^a ; He Zhao^b ; Yu Chao^a ; Zhuang Liu^a ; ^{zliu@suda.edu.cn" class="auth_mail" title="E-mail the corresponding author}
• 关键词：CaCO3 nanoparticle ; pH-sensitive ; MR imaging ; Real-time monitoring ; Cancer combination therapy
• 刊名：Biomaterials
• 出版年：2016
• 出版时间：December 2016
• 年：2016
• 卷：110
• 期：Complete
• 页码：60-70
• 全文大小：3454 K

文摘

The exploration of stimuli-responsive nano-theranostics provides powerful tools for simultaneously enhancing the accuracy and efficiency of cancer therapies. Herein, we develop mono-dispersed CaCO₃ nanoparticles modified with polyethylene glycol (PEG) as a multifunctional nano-carrier for efficient loading of both Mn²⁺-chelated chlorin e6 (Ce6(Mn)) as a photosensitizer, and doxorubicin (DOX) as a chemotherapy drug. Our CaCO₃@Ce6(Mn)-PEG(DOX) nanoparticles, while being stable under physiological pH at 7.4, appear to be highly sensitive to reduced pH and would be rapidly degraded under slightly acidic environment, effectively releasing loaded therapeutic agents. Interestingly, owing to released Ce6(Mn), those nanoparticles show an interesting pH-dependent T1 signal enhancement under magnetic resonance (MR) imaging, which could be utilized for real-time monitoring of drug release. As discovered by MR and fluorescence imaging, intravenously (i.v.) injected CaCO₃@Ce6(Mn)/DOX-PEG could gradually accumulate in the tumor, contributing to a superior synergistic anti-tumor effect in the combined photodynamic & chemotherapy. In conclusion, we have developed a tumor-pH-activated nanocarrier based on biodegradable CaCO₃ nanoparticles, which may be an ideal cancer theranostic nanoplatform with substantial potential for future clinical translation.